Effects of a short-chain phospholipid on ion transport pathways in rabbit nasal airway epithelium

Am J Physiol. 1996 Oct;271(4 Pt 1):L646-55. doi: 10.1152/ajplung.1996.271.4.L646.

Abstract

We investigated the mechanism of interference of mucosal application of the short-chain phospholipid didecanoyl-L-alpha-phosphatidylcholine (DDPC; 0.1-0.5%) with ion transport pathways in isolated rabbit nasal airway epithelium (RNAE). Transports of Na+ and Cl- were evaluated from tracer ion fluxes, short-circuit current (Isc), and epithelial conductance (Gt) under short-circuit conditions in Ussing chambers. DDPC rapidly and reversibly abolished net Na+ absorption, reduced control Isc (approximately 110 microA/cm2) by approximately 80%, and induced a small Cl secretion. Intracellular Ca2+ concentration ([Ca2+]i) increased dose dependently and transiently (measured by fura 2 in cultured rabbit airway epithelium), but ionomycin failed to mimic the decrease in Isc. The rise in [Ca2+]i may explain a Ba(2+)-sensitive transient activation of a basolateral K+ conductance. Indomethacin-sensitive prostaglandin E2 production in RNAE increased severalfold, but cyclooxygenase and lipoxygenase inhibitors did not prevent DDPC-induced changes in Isc. DDPC initially decreased control Gt (approximately 13 mS/cm2) by approximately 25% due to inhibition of amiloride-sensitive Na+ channels, and then reversibly increased Gt to approximately 45% above control values. Passive Na+ fluxes increased more than Cl fluxes, suggesting that the increase in Gt is due to formation of a paracellular shunt conductance in parallel with unaffected, anion-selective tight junction channels. The results suggest that DDPC inhibits apical membrane Na+ channels and causes structural changes in tight junctions after incorporation in apical cell membranes.

MeSH terms

  • Animals
  • Biological Transport / drug effects
  • Cells, Cultured
  • Dinoprostone / metabolism
  • Electric Conductivity
  • Epithelium / metabolism
  • Female
  • Membrane Potentials
  • Nasal Mucosa / drug effects
  • Nasal Mucosa / metabolism*
  • Phosphatidylcholines / pharmacology*
  • Rabbits
  • Sodium / physiology*
  • Sodium Channel Blockers*

Substances

  • Phosphatidylcholines
  • Sodium Channel Blockers
  • 1,2-didecanoylphosphatidylcholine
  • Sodium
  • Dinoprostone